Visitor Monitoring Drug Details: ACCUTANE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Drug Details

Drug Name: ACCUTANE
FDA Application No: (NDA) 018662
Active Ingredient(s): ISOTRETINOIN
Company: HLR
Original Approval or Tentative Approval Date: May 7, 1982
Chemical Type: 1 New molecular entity (NME)
Review Classification: P Priority review drug
 
Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
ACCUTANE ISOTRETINOIN10MGCAPSULE; ORAL Prescription No AB
ACCUTANE ISOTRETINOIN40MGCAPSULE; ORAL Prescription Yes AB
ACCUTANE ISOTRETINOIN20MGCAPSULE; ORAL Prescription Yes AB


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